| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37739503_37739577del | CA913190793 | HNF1B | c.410_484del (p.Arg137_Lys161del) | ClinVar |
| 17 | g.37739571T>A | CA398751538 | HNF1B | c.413A>T (p.Glu138Val) | |
| 17 | g.37739571T>C | CA398751539 | HNF1B | c.413A>G (p.Glu138Gly) | |
| 17 | g.37739571T>G | CA398751540 | HNF1B | c.413A>C (p.Glu138Ala) | |
| 17 | g.37739572C>A | CA398751541 | HNF1B | c.412G>T (p.Glu138Ter) | |
| 17 | g.37739572C>G | CA398751543 | HNF1B | c.412G>C (p.Glu138Gln) | |
| 17 | g.37739572C>T | CA398751545 | HNF1B | c.412G>A (p.Glu138Lys) | |
| 17 | g.37739573C>A | CA398751546 | HNF1B | c.411G>T (p.Arg137Ser) | |
| 17 | g.37739573C>G | CA398751548 | HNF1B | c.411G>C (p.Arg137Ser) | |
| 17 | g.37739573C>T | CA499603959 | HNF1B | c.411G>A (p.Arg137=) | |
| 17 | g.37739574C>A | CA398751549 | HNF1B | c.410G>T (p.Arg137Met) | |
| 17 | g.37739574C>G | CA398751551 | HNF1B | c.410G>C (p.Arg137Thr) | |
| 17 | g.37739574C>T | CA398751552 | HNF1B | c.410G>A (p.Arg137Lys) | ClinVar dbSNP gnomAD v4 |
| 17 | g.37739575T>A | CA398751554 | HNF1B | c.409A>T (p.Arg137Trp) | |
| 17 | g.37739575T>C | CA398751555 | HNF1B | c.409A>G (p.Arg137Gly) | |
| 17 | g.37739575T>G | CA499603960 | HNF1B | c.409A>C (p.Arg137=) | |
| 17 | g.37739576C>A | CA398751557 | HNF1B | c.408G>T (p.Gln136His) | |
| 17 | g.37739576C>G | CA398751559 | HNF1B | c.408G>C (p.Gln136His) | |
| 17 | g.37739576C>T | CA499603961 | HNF1B | c.408G>A (p.Gln136=) | |
| 17 | g.37739577T>A | CA398751561 | HNF1B | c.407A>T (p.Gln136Leu) | |
| 17 | g.37739577T>C | CA398751562 | HNF1B | c.407A>G (p.Gln136Arg) | |
| 17 | g.37739577T>G | CA398751564 | HNF1B | c.407A>C (p.Gln136Pro) | |
| 17 | g.37739578G>A | CA398751565 | HNF1B | c.406C>T (p.Gln136Ter) | ClinVar |
| 17 | g.37739578G>C | CA398751567 | HNF1B | c.406C>G (p.Gln136Glu) | ClinVar |
| 17 | g.37739578G>T | CA398751568 | HNF1B | c.406C>A (p.Gln136Lys) | |
| 17 | g.37739582dup | CA10603444 | HNF1B | c.406dup (p.Gln136ProfsTer?) | ClinVar dbSNP |
| 17 | g.37739579G>A | CA499603962 | HNF1B | c.405C>T (p.Pro135=) | |
| 17 | g.37739579G>C | CA499603963 | HNF1B | c.405C>G (p.Pro135=) | |
| 17 | g.37739579G>T | CA499603964 | HNF1B | c.405C>A (p.Pro135=) | |
| 17 | g.37739580G>A | CA398751570 | HNF1B | c.404C>T (p.Pro135Leu) | |
| 17 | g.37739580G>C | CA398751572 | HNF1B | c.404C>G (p.Pro135Arg) | |
| 17 | g.37739580G>T | CA398751573 | HNF1B | c.404C>A (p.Pro135His) | |
| 17 | g.37739581G>A | CA398751578 | HNF1B | c.403C>T (p.Pro135Ser) | |
| 17 | g.37739581G>C | CA398751577 | HNF1B | c.403C>G (p.Pro135Ala) | |
| 17 | g.37739581G>T | CA398751575 | HNF1B | c.403C>A (p.Pro135Thr) | |
| 17 | g.37739582G>A | CA499603965 | HNF1B | c.402C>T (p.Ile134=) | ClinVar dbSNP gnomAD v4 |
| 17 | g.37739582G>C | CA398751580 | HNF1B | c.402C>G (p.Ile134Met) | |
| 17 | g.37739582G>T | CA499603966 | HNF1B | c.402C>A (p.Ile134=) | gnomAD v4 |
| 17 | g.37739583A>C | CA398751585 | HNF1B | c.401T>G (p.Ile134Ser) | |
| 17 | g.37739583A>G | CA398751582 | HNF1B | c.401T>C (p.Ile134Thr) | |
| 17 | g.37739583A>T | CA398751583 | HNF1B | c.401T>A (p.Ile134Asn) | ClinVar dbSNP |
| 17 | g.37739584T>A | CA398751587 | HNF1B | c.400A>T (p.Ile134Phe) | |
| 17 | g.37739584T>C | CA398751589 | HNF1B | c.400A>G (p.Ile134Val) | |
| 17 | g.37739584T>G | CA398751590 | HNF1B | c.400A>C (p.Ile134Leu) | |
| 17 | g.37739585G>A | CA499603967 | HNF1B | c.399C>T (p.Asn133=) | dbSNP |
| 17 | g.37739585G>C | CA398751591 | HNF1B | c.399C>G (p.Asn133Lys) | |
| 17 | g.37739585G>T | CA398751593 | HNF1B | c.399C>A (p.Asn133Lys) | |
| 17 | g.37739586T>A | CA398751595 | HNF1B | c.398A>T (p.Asn133Ile) | |
| 17 | g.37739586T>C | CA398751597 | HNF1B | c.398A>G (p.Asn133Ser) | ClinVar |
| 17 | g.37739586T>G | CA398751598 | HNF1B | c.398A>C (p.Asn133Thr) |